Peter G. Czarnecki

Blood Pressure in Early Autosomal Dominant Polycystic Kidney Disease

Robert W. Schrier, Kaleab Z. Abebe, Ronald D. Perrone et al. · New England Journal of Medicine · 2014 · 504 citations · Full text

Angiotensin Blockade in Late Autosomal Dominant Polycystic Kidney Disease

Vicente E. Torres, Kaleab Z. Abebe, Arlene B. Chapman et al. · New England Journal of Medicine · 2014 · 278 citations · Full text

Defects in the IFT-B Component IFT172 Cause Jeune and Mainzer-Saldino Syndromes in Humans

Jan Halbritter, Albane A. Bizet, Miriam Schmidts et al. · The American Journal of Human Genetics · 2013 · 225 citations · Full text

Ciliary and centrosomal defects associated with mutation and depletion of the Meckel syndrome genes MKS1 and MKS3

Rachaneekorn Tammachote, Cynthia J. Hommerding, Rachel M. Sinders et al. · Human Molecular Genetics · 2009 · 121 citations · Full text

Developmental Biology, Mendelian Disorder, Cell Division +15

B9D1 is revealed as a novel Meckel syndrome (MKS) gene by targeted exon-enriched next-generation sequencing and deletion analysis

Katharina Hopp, Christina M. Heyer, Cynthia J. Hommerding et al. · Human Molecular Genetics · 2011 · 88 citations · Full text